key: cord-0929708-1nq7892g authors: Barry, Aisling; Mina, Daniel Santa; Langelier, David M.; Wong, Philip; Anne Koch, C. title: Supporting an Athlete With Breast Cancer: A Case Report date: 2022-02-07 journal: J Patient Exp DOI: 10.1177/23743735221077539 sha: 0a10b718aa8de946421a83635d5eb40c1aeddb3b doc_id: 929708 cord_uid: 1nq7892g For cancer survivors who also identify as athletes, a rigorous exercise that was once part of their daily routine and fundamental to their physical, psychological, and potentially financial well-being, may be temporarily or permanently altered in ways that exacerbate cancer-related changes in quality of life. This report presents an illustrative case of an endurance athlete who underwent breast cancer treatment and her subsequent return to high-performance, high elevation sport. We identify gaps in oncology research and patient educational tools to counsel athletes with cancer regarding the acute and long-term effects of cancer treatment and possibility of returning to a precancer level of fitness and performance. The report also highlights the need to tailor individualized cancer care treatment, rehabilitation, and the ability to preempt potential clinical and psychological side effects that may substantially impact training and competition. As an endurance athlete and high-altitude mountain climber, I am used to discomfort. In fact, I crave it on some level, as it builds my tolerance to cold, lack of oxygen, pain, and refreshes my spirit of physicality and resilience. Even with the discomfort, I must perform at the highest level in order to succeed, indeed, to survive. For high-performance athletes, training and competition are fundamental to their identity and quality of life (1) . Cancer and associated treatments are often deleterious to physical and mental health, consequently undermining the capacity of athletes to prepare and perform at precancer levels (2) . Breast cancer treatment toxicities are welldocumented (3) and may result in a number of physical, physiological, and psychological acute and late side effects (4) . The iCanCare survey (5) of patients with early stage breast cancer reported substantial treatment-associated toxicities and related burden due to their cancer treatment. Exercise and physical activity have shown to improve and combat many cancer treatment-related side effects with benefits observed in exercise tolerance, strength, endurance, and psychology (6) . This report presents an illustrative case of the experiences and perspectives of a competitive mountain climber and endurance athlete who underwent breast cancer treatment and her subsequent return to sport. As per institutional guidelines, research ethics board approval was not required for this case report. Verbal and written informed consent were obtained from the patient for the use of anonymized information and her direct contribution to the patient experience portion of this report (patient quotes in italics). Upon learning that I had cancer, my initial reaction was not fear, rather I was concerned about how it would impact my expedition schedule and set back my physical strength and conditioning. This 42-year-old female with a background in elite, highaltitude mountain climbing, has set many national and international records. After self-identifying a lump in her right breast, she underwent further evaluation and was diagnosed with an early stage breast cancer measuring 2.8 cm, grade 3, estrogen/progesterone receptor-negative, and human epidermal growth factor receptor 2 positive without evidence of abnormal lymph nodes or metastatic disease (clinical stage T2N0M0 (IIA)). Her physical examination was otherwise unremarkable. She had no significant past medical history or genetic predisposition to breast cancer and was not taking any medications. The patient received neoadjuvant fluorouracil-epirubicincyclophosphamide then docetaxel chemotherapy, with trastuzumab (prescribed for 12-month total) combined with pertuzumab, followed by a right breast lumpectomy and sentinel lymph node biopsy (pathology yielded residual 0.1 mm of ductal carcinoma in situ (pathological stage ypTisN0)). The patient received adjuvant breast-alone radiotherapy ( Figure 1 , Radiotherapy Plan; Figure 2 , Timeline of Events). The patient underwent a regular clinical review of symptoms, including cardiac monitoring with 2D/3D echocardiograms (ECHO) as part of routine follow-up for her anthracycline and trastuzumab systemic therapies. The 6-month ECHO showed a 9% decrease (67%-58%) in left ventricular ejection fraction (LVEF) from baseline (pre neoadjuvant chemotherapy), but still within the normal range (50%-70%). Her global longitudinal strain (a measure of left ventricular systolic function) had fallen from −22.5% to −16.5% (normal >−18%, borderline −16% to −18% (7)). At 12 months post baseline, LVEF continued to be within normal range at 53%, and longitudinal strain recovered to within normal limits (−18.7%). Throughout the period of treatment, she experienced minimal reduction in energy and transient skin erythema during radiotherapy with no reported shortness of breath or worsening of quality of life. My challenges with the treatment were specific to concerns about lymphedema and its impact on my future as an athlete. I shared my concerns with each of my doctors and care professionals, and I was met with compassion and understanding. Throughout neoadjuvant and adjuvant treatments, the patient maintained a self-administered regular aerobic and resistance-based training schedule, consisting of a weekly combination of running, walking, rowing, stepping, and biking (Table 1) , with a weighted vest, and both free weight and body weight supported exercises targeting large muscle groups (i.e., quadriceps, hamstrings etc.). Following radiotherapy, her fitness goal shifted to progress her aerobic and resistance capacity for a return to high-altitude climbing. As I progressed through treatment and I learned more about the potential negative outcomes, I had two memorable occasions when fear gripped my heart and soul as I was faced with the realization that this experience might actually alter my quality of life and continued athleticism. On the whole, however, I remained very positive about the outcome, and I believed that I would find myself in the mountains again. I continued to train as much as my body would allow, and I envisioned climbing toward a high mountain summit as motivation. On completion of radiotherapy, the patient was referred to cancer rehabilitation and survivorship program for exercise clearance as she aimed to complete high-altitude climbs to 5600 meters and 6800 meters within 8 weeks and at 13 weeks post-radiotherapy, respectively. Her primary rehabilitation team was made up of a physical medicine and rehabilitation specialist (physiatrist), physiotherapist, and kinesiologist with advanced training in clinical exercise physiology. Given the lack of evidence surrounding the safety of highaltitude exercise post cancer treatment and the potential toxicities of her chemotherapy and radiation therapies, she was referred for further cardiac and respiratory testing to better predict cardiorespiratory stress at elevation in the absence of clear testing guidelines. A high-altitude stimulation test was performed 4 weeks post-radiotherapy assessing her respiratory function status, potential hypoxia, and the impact on cardiac strain at elevations similar to her intended climbs. During the test, she demonstrated expected alveolar hyperventilation, adequate arterial oxygenation on arterial blood gas measures, and no desaturations of the fraction of inspired oxygen (FiO 2 ) at 15% oxygen. The patient subsequently underwent a cardiopulmonary exercise test using an electronically braked cycle ergometer with electrocardiogram and gas analysis using a ramp protocol. The duration of the test was 15 min and 1 s and the patient achieved an absolute VO 2 peak (maximum rate of oxygen consumption unadjusted for body mass) of 2.48 LO 2 /min, and a relative VO 2 peak of 36.6 mL O 2 /kg body weight/min. At test termination, the patient reported a rating of perceived exertion of 9/10 and her respiratory exchange ratio was 1.14, with an estimated anaerobic threshold occurring at a heart rate of 150 beats per minute ( Figure 3A and B ). There were no medical complications or concerns over the course of the test. With the rehabilitation team, I felt that I was working with practitioners who appreciated the uniqueness of my situation and were curious about the impact of cancer treatment on a high-altitude mountain climber. The patient successfully reached the summit of the 5600-meter climb at 8 weeks post radiotherapy, followed April 3 3 Nil 49 9 May 3 6 3 28 9 June 3 3 3 21 15 Chemotherapy end July 3 3 6 21 12 Surgery August Nil 3 Nil 49 15 September 3 9 Nil 28 15 Radiotherapy start October 3 6 Nil 28 12 Radiotherapy end November 3 6 Nil 35 15 December 3 3 9 21 15 2020 January 5600 meter climb February 6800 meter climb March COVID-19 pandemic declared by a 6800-meter climb at 13 weeks post radiotherapy. Upon post-climb follow-up, she reported mild difficulties with acclimatization based on the timing of her climb, denying any significant or long-lasting respiratory symptoms. A post climb cardiorespiratory fitness test was planned but eventually canceled due to the COVID-19 pandemic. The patient remains under ongoing follow-up with the oncology and rehabilitation teams. Breast cancer treatment toxicities are well-documented (3) and may result in a number of physical, physiological, and psychological acute and late adverse effects (4). The importance of physical activity and exercise in cancer prevention and in pre and post cancer treatment rehabilitation is increasing among patients and physicians, as multiple studies show an improvement in cancer-related side effects and potential survival benefits (1-6). High-intensity exercise may be achievable and safe during and after cancer treatment and may mitigate or recover deteriorations in physical functioning and worsening symptoms better than low or moderate intensity (8, 9) . A large body of evidence highlights the cardiotoxic effects of breast cancer treatment and subsequent reductions in aerobic performance (10) (11) (12) (13) ; however, there is a paucity of data specifically assessing this in cancer patients who identify as athletes (14) . Decreased LVEF and myocyte injury are known causes of cardiac dysfunction (15) and often assessed using aerobic capacity measurements (as low VO 2 max has been associated with poorer cardiovascular outcomes) assessing global cardiac and respiratory function (16) . Given the aerobic demands of high-altitude mountain climbing and the known adverse effects of the patient's treatment, cardiorespiratory assessments were prioritized for the patient in the presented case to determine safety and physiological capacity for such events. The patient had a small decline in her LVEF during her neoadjuvant chemotherapy; however, this remained within the normal range and her longitudinal strain recovered. Similarly, her pre-climb aerobic fitness (as measured by cardiopulmonary exercise test) was consistent with reference data from females of a similar age without cardiovascular disease (17) . In addition to the potential physical effects of cancer treatment in athletes, long-term adverse psychological effects may occur, such as trauma of diagnosis, loss of identity, deficits in role, emotional, cognitive, and social functioning (18) . For some athletes, this may result in a transition to reduced activity or even involuntary retirement. The athlete described in this case report did not describe acute or chronic deficits in role, cognitive, or social functioning; however, these were not formally assessed with validated quality of life measurement tools. Involvement of a health professional specializing in sport psychology may be warranted to support a patient as they navigate a return to sport or the temporary or permanent cessation of competitive activity. Lessons Learned: 1. Identifying people with cancer who are also highperformance athletes is relevant to preserving physical, mental, and vocational functions related to their sport. 2. Consideration of additional evaluation of physiological and functional health markers (e.g., cardiorespiratory fitness, muscle mass, and strength), to minimize the impact on performance and time off from training is warranted 3. Capitalizing on advancing technology, such as remote telemonitoring, fitness biometrics, and artificial intelligence, may present us with an opportunity to understand such physiological changes in an athlete's performance following a cancer diagnosis and during and after their cancer treatment. 4. The psychological impact of cancer and its treatment for athlete's may be different than those whose identity is not entrenched with sport-related performance concerns. Pre-empting and managing the potential psychological challenges of athletes who must temporarily or permanently discontinue training and competition is advisable. A growing number of cancer patients who are athletes are being identified. Additional prospective studies are required to achieve a more personalized treatment approach that aims to maintain or mitigate deleterious effects on sport performance. My experience through the disease process was relatively positive, in that I always understood what was to happen to me, and I felt that I had excellent care and treatment. The doctors were patient with my many questions and they allowed me time to research and make thoughtful decisions. I felt supported and heard. 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The authors would also like to acknowledge the Princess Margaret Cancer Foundation. Conceptualization, A.B., D.SM., and C.A.K.; methodology, all authors; writing-original draft preparation, A.B.; writingreview and editing, all authors. All authors have read and agreed to the published version of the manuscript. All procedures were conducted as per standard of care policies, therefore not requiring further research ethics board approval. Verbal and written informed consent was obtained from the patient for their anonymized information and their direct contribution to the patient experience portion of the report published in this article. The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. The author(s) received no financial support for the research, authorship, and/or publication of this article. Aisling Barry https://orcid.org/0000-0003-1587-669X David M. Langelier https://orcid.org/0000-0002-9863-5084